- Trials with a EudraCT protocol (175)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
175 result(s) found for: Joint replacement.
Displaying page 1 of 9.
EudraCT Number: 2007-007813-35 | Sponsor Protocol Number: TBA | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:University Hospital of North Tees and Hartlepool | |||||||||||||
Full Title: Randomised Controlled Trial of the Use of Topical Application of Tranexamic Acid in Primary Cemented Total Knee Replacement (TRANX-K). | |||||||||||||
Medical condition: In this study Tranexamic acid efficacy in reducing blood loss will be investigated in total knee replacement.Tranexamic acid will be applied topically to the exposed tissue around the knee joint pr... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001299-19 | Sponsor Protocol Number: GJNH-06-01 | Start Date*: 2006-05-12 |
Sponsor Name:Golden Jubilee National Hospital | ||
Full Title: Prospective randomised trial comparing intraoperative topical Quixil and intravenous tranexamic acid in reduction of blood loss following primary hip and knee joint replacement surgery | ||
Medical condition: Elective total knee replacement and total hip replacement. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005471-10 | Sponsor Protocol Number: 4745 | Start Date*: 2009-06-17 | |||||||||||
Sponsor Name:Nina Olofsson | |||||||||||||
Full Title: Plasma concentration of Ropivacain and Ketorolac after local infiltration during surgery in hip replacement during the first 24 postoperative hours. | |||||||||||||
Medical condition: Postoperative pain after surgery for hip replacement. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003395-23 | Sponsor Protocol Number: HK_VL_08_2014 | Start Date*: 2015-01-20 | |||||||||||
Sponsor Name:Section for Surgical Pathophysiology, Rigshospitalet | |||||||||||||
Full Title: Effect of preoperative intravenous highdose methylprednisolone on quadriceps muscle function, endothelial function, complement activation and glucose homeostasis in patients scheduled for total kne... | |||||||||||||
Medical condition: Knee joint arthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002744-40 | Sponsor Protocol Number: HK_EA_02_2014 | Start Date*: 2014-09-23 | |||||||||||
Sponsor Name:Section For Surgical Pathophysiology, Rigshospitalet | |||||||||||||
Full Title: Preoperative intraarticular injection of methylprednisolone, in patients scheduled for total knee-arthroplasty | |||||||||||||
Medical condition: Knee joint arthrosis with hyperalgesia and severe movement related pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000102-19 | Sponsor Protocol Number: HL_VL_01_2015 | Start Date*: 2015-07-07 | |||||||||||
Sponsor Name:Section for Surgical Pathophysiology, Rigshospitalet | |||||||||||||
Full Title: Effect of preoperative intravenous highdose methylprednisolone on orthostatic intolerance, sleeping pattern, glucose homeostasis and immune signaling in patients scheduled for total hip-arthroplasty | |||||||||||||
Medical condition: Hip joint arthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000107-94 | Sponsor Protocol Number: RB15.005 | Start Date*: 2015-03-25 | |||||||||||
Sponsor Name:CHRU de Brest | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012043-42 | Sponsor Protocol Number: RSCH 01/10 | Start Date*: 2011-07-11 | ||||||||||||||||
Sponsor Name:Royal Surrey County Hospital NHS Trust | ||||||||||||||||||
Full Title: The Effect of a Human Surgical Sealant on Range of Motion in Total Knee Replacement | ||||||||||||||||||
Medical condition: Use of human surgical sealant during total knee replacement and if this affects knee movement for the 1st year after surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000926-21 | Sponsor Protocol Number: AMSC-BDT-002 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name:Fakultní nemocnice Hradec Králové | |||||||||||||
Full Title: Innovation of method cryopreservation for clinical use autologous multipotent mesenchymal stem cells (MSCs) for treatment of extensive skeletal defects in revision surgery of total hip arthroplasty+ | |||||||||||||
Medical condition: Revision total hip arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003169-33 | Sponsor Protocol Number: 2013-578 | Start Date*: 2013-10-30 | |||||||||||
Sponsor Name:Anders Troelsen | |||||||||||||
Full Title: Evaluation of intra articular Tranexamic acid for reduction of total blood loss in total knee unilateral arthroplasty | |||||||||||||
Medical condition: The benefit of additional Tranexamic Acid (TXA) injected intra-articular at the end of surgery for patients undergoing a unilateral total knee arthroplasty in addition to conventional IV TXA to red... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002635-23 | Sponsor Protocol Number: NBF_HK_02_2018. | Start Date*: 2018-10-23 | ||||||||||||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark. | ||||||||||||||||||||||||||||
Full Title: Highdose steroids in High Pain Responders undergoing total knee-arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||||||||||||
Medical condition: Perioperative management of a group of High Pain Responders in total knee-arthroplasty because of kneeosteoarthritis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003730-10 | Sponsor Protocol Number: 001-2014-KHTY | Start Date*: 2014-12-01 | ||||||||||||||||
Sponsor Name:Department of Anesthesiology, Næstved Hospital | ||||||||||||||||||
Full Title: Effect of a lateral nerve of the thigh block on post-operative pain among patients with pain (VAS>40mm) during flexion of the hip the first or second postoperative day | ||||||||||||||||||
Medical condition: Pain after total hip replacement surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000628-14 | Sponsor Protocol Number: ISS20109714 | Start Date*: 2013-09-13 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Denosumab in enhancement of bone bonding of hip prosthesis in postmenopausal women: a randomized, double-blind, placebo-controlled study | |||||||||||||
Medical condition: Hip osteoarthritis | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000126-39 | Sponsor Protocol Number: 07-127 | Start Date*: 2008-05-26 | |||||||||||
Sponsor Name:CHU de Caen | |||||||||||||
Full Title: Analgésie post-opératoire pour prothèse totale de genou par cathéter péri-nerveux fémoral: Etude comparative de la levobupivacaine 0,125% versus ropivacaine 0, 2%. Protocole LPTG | |||||||||||||
Medical condition: Prothèse totale du genou | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002170-39 | Sponsor Protocol Number: Knemo01 | Start Date*: 2017-09-14 | |||||||||||
Sponsor Name:Eksote | |||||||||||||
Full Title: Combination of intrathecal morphine and local infiltration analgesia in treatment postoperative pain of total knee arthroplasty | |||||||||||||
Medical condition: Postoperative pain after total knee arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001511-20 | Sponsor Protocol Number: 1 | Start Date*: 2017-01-19 |
Sponsor Name:Institute for Pharmacology and Toxicology | ||
Full Title: Pharmacokinetica of Cefuroxime | ||
Medical condition: hip or knee replacement or spine bone surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003756-37 | Sponsor Protocol Number: ANT-005 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:Anthos Therapeutics | |||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Blinded Endpoint Evaluation, Active-Controlled, Dose-Ranging Study to Compare the Efficacy and Safety of i.v. MAA868 and s.c. Enoxaparin in Adult Patients Und... | |||||||||||||
Medical condition: Elective unilateral total knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) BE (Completed) LV (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003051-37 | Sponsor Protocol Number: 2013-07-03 | Start Date*: 2013-08-28 | ||||||||||||||||
Sponsor Name:Kuopion yliopistollinen sairaala | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001214-10 | Sponsor Protocol Number: AAUH-01-2015 | Start Date*: 2015-06-02 | ||||||||||||||||
Sponsor Name:Aalborg universitets hospital [...] | ||||||||||||||||||
Full Title: Analgetic effect of perioperative klorzoxazon at total hip or knee arthroplasty | ||||||||||||||||||
Medical condition: Perioperative pain after incertion of hip or knee arthroplasty | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000692-14 | Sponsor Protocol Number: HKO-22112010 | Start Date*: 2011-11-03 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Hannu Kokki | ||||||||||||||||||||||||||||||||||||||
Full Title: | ||||||||||||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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